Canonical Allele Identifier: PA1139705132
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 857052
ClinVar RCV Id: RCV001062653 RCV002429698
ClinVar Variation Id: 1503604
ClinVar RCV Id: RCV002045469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ser838Arg
CA396472246
NM_004360.5:c.2512A>C
CA396472258
NM_004360.5:c.2514C>A
CA396472260
NM_004360.5:c.2514C>G